FERNANDEZ-VIZARRA BAILEY, ERIKA MARIA
FERNANDEZ-VIZARRA BAILEY, ERIKA MARIA
Dipartimento di Scienze Biomediche - DSB
A homozygous MRPL24 mutation causes a complex movement disorder and affects the mitoribosome assembly
2020 Di Nottia, Michela; Marchese, Maria; Verrigni, Daniela; Mutti, Christian Daniel; Torraco, Alessandra; Oliva, Romina; Fernandez-Vizarra, Erika; Morani, Federica; Trani, Giulia; Rizza, Teresa; Ghezzi, Daniele; Ardissone, Anna; Nesti, Claudia; Vasco, Gessica; Zeviani, Massimo; Minczuk, Michal; Bertini, Enrico; Santorelli, Filippo Maria; Carrozzo, Rosalba
APOPT1/COA8 assists COX assembly and is oppositely regulated by UPS and ROS
2019 Signes, Alba; Cerutti, Raffaele; Dickson, Anna S; Benincá, Cristiane; Hinchy, Elizabeth C; Ghezzi, Daniele; Carrozzo, Rosalba; Bertini, Enrico; Murphy, Michael P; Nathan, James A; Viscomi, Carlo; Fernandez-Vizarra, Erika; Zeviani, Massimo
Assembly of mammalian oxidative phosphorylation complexes I-V and supercomplexes
2018 Signes, Alba; Fernandez-Vizarra, Erika
Assembly of the oxidative phosphorylation system in humans: what we have learned by studying its defects
2009 Fernández-Vizarra, Erika; Tiranti, Valeria; Zeviani, Massimo
Biallelic mutations in NDUFA8 cause complex I deficiency in two siblings with favorable clinical evolution
2020 Tort, Frederic; Barredo, Estibaliz; Parthasarathy, Ranjani; Ugarteburu, Olatz; Ferrer-Cortès, Xenia; García-Villoria, Judit; Gort, Laura; González-Quintana, Adrián; Martín, Miguel A; Fernández-Vizarra, Erika; Zeviani, Massimo; Ribes, Antonia
Bioenergetic consequences from xenotopic expression of a tunicate AOX in mouse mitochondria: Switch from RET and ROS to FET
2020 Szibor, Marten; Gainutdinov, Timur; Fernandez-Vizarra, Erika; Dufour, Eric; Gizatullina, Zemfira; Debska-Vielhaber, Grazyna; Heidler, Juliana; Wittig, Ilka; Viscomi, Carlo; Gellerich, Frank; Moore, Anthony L
Cavitating Leukoencephalopathy With Posterior Predominance Caused by a Deletion in the APOPT1 Gene in an Indian Boy
2018 Sharma, Suvasini; Singh, Preeti; Fernandez-Vizarra, Erika; Zeviani, Massimo; Van der Knaap, Marjo S; Saran, Ravindra Kumar
CEDAR, an online resource for the reporting and exploration of complexome profiling data
2021 van Strien, Joeri; Haupt, Alexander; Schulte, Uwe; Braun, Hans-Peter; Cabrera-Orefice, Alfredo; Choudhary, Jyoti S; Evers, Felix; Fernandez-Vizarra, Erika; Guerrero-Castillo, Sergio; Kooij, Taco W A; Páleníková, Petra; Pardo, Mercedes; Ugalde, Cristina; Wittig, Ilka; Wöhlbrand, Lars; Brandt, Ulrich; Arnold, Susanne; Huynen, Martijn A
CG7630 is the Drosophila melanogaster homolog of the cytochrome c oxidase subunit COX7B
2022 Brischigliaro, Michele; Cabrera-Orefice, Alfredo; Sturlese, Mattia; Elurbe, Dei M; Frigo, Elena; Fernandez-Vizarra, Erika; Moro, Stefano; Huynen, Martijn A; Arnold, Susanne; Viscomi, Carlo; Zeviani, Massimo
COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiency
2016 Martinez Lyons, Anabel; Ardissone, Anna; Reyes, Aurelio; Robinson, Alan J; Moroni, Isabella; Ghezzi, Daniele; Fernandez-Vizarra, Erika; Zeviani, Massimo
Cooperative assembly of the mitochondrial respiratory chain
2022 Fernández-Vizarra, Erika; Ugalde, Cristina
COX7A2L Is a Mitochondrial Complex III Binding Protein that Stabilizes the III2+IV Supercomplex without Affecting Respirasome Formation
2016 Pérez-Pérez, Rafael; Lobo-Jarne, Teresa; Milenkovic, Dusanka; Mourier, Arnaud; Bratic, Ana; García-Bartolomé, Alberto; Fernández-Vizarra, Erika; Cadenas, Susana; Delmiro, Aitor; García-Consuegra, Inés; Arenas, Joaquín; Martín, Miguel A; Larsson, Nils-Göran; Ugalde, Cristina
Defective PITRM1 mitochondrial peptidase is associated with Aβ amyloidotic neurodegeneration
2016 Brunetti, Dario; Torsvik, Janniche; Dallabona, Cristina; Teixeira, Pedro; Sztromwasser, Pawel; Fernandez-Vizarra, Erika; Cerutti, Raffaele; Reyes, Aurelio; Preziuso, Carmela; D'Amati, Giulia; Baruffini, Enrico; Goffrini, Paola; Viscomi, Carlo; Ferrero, Ileana; Boman, Helge; Telstad, Wenche; Johansson, Stefan; Glaser, Elzbieta; Knappskog, Per M; Zeviani, Massimo; Bindoff, Laurence A
Duplexing complexome profiling with SILAC to study human respiratory chain assembly defects
2021 Páleníková, Petra; Harbour, Michael E; Prodi, Federica; Minczuk, Michal; Zeviani, Massimo; Ghelli, Anna; Fernández-Vizarra, Erika
Editorial: Mitochondrial OXPHOS System: Emerging Concepts and Technologies and Role in Disease
2022 Fernández-Vizarra, Erika; Callegari, Sylvie; Garrabou, Glòria; Pacheu-Grau, David
Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene
2016 Bianciardi, Laura; Imperatore, Valentina; Fernandez-Vizarra, Erika; Lopomo, Angela; Falabella, Micol; Furini, Simone; Galluzzi, Paolo; Grosso, Salvatore; Zeviani, Massimo; Renieri, Alessandra; Mari, Francesca; Frullanti, Elisa
FASTKD2 nonsense mutation in an infantile mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency
2008 Ghezzi, Daniele; Saada, Ann; D'Adamo, Pio; Fernandez-Vizarra, Erika; Gasparini, Paolo; Tiranti, Valeria; Elpeleg, Orly; Zeviani, Massimo
Five entry points of the mitochondrially encoded subunits in mammalian complex I assembly
2010 Perales-Clemente, Ester; Fernández-Vizarra, Erika; Acín-Pérez, Rebeca; Movilla, Nieves; Bayona-Bafaluy, María Pilar; Moreno-Loshuertos, Raquel; Pérez-Martos, Acisclo; Fernández-Silva, Patricio; Enríquez, José Antonio
How do human cells react to the absence of mitochondrial DNA?
2009 Mineri, Rossana; Pavelka, Norman; Fernandez-Vizarra, Erika; Ricciardi-Castagnoli, Paola; Zeviani, Massimo; Tiranti, Valeria
Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathy
2007 Fernandez-Vizarra, Erika; Bugiani, Marianna; Goffrini, Paola; Carrara, Franco; Farina, Laura; Procopio, Elena; Donati, Alice; Uziel, Graziella; Ferrero, Iliana; Zeviani, Massimo